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Nicotinamide-Induced Apoptosis Can Be Enhanced by Melatonin in Mouse Myeloma Cells

机译:褪黑素可以增强小鼠骨髓瘤细胞中烟酰胺诱导的细胞凋亡。

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The mechanism of apoptosis induced by nicotinamide was investigated by treating mouse myeloma cells (Sp2/0) with various concentrations of nicotinamide. The typical hallmarks of apoptosis, including chromatin condensation and DNA fragmentation, were detected when cells were treated with nicotinamide at concentrations of 30, 40, 50, and 60 mmol/L. The apoptosis percentage increased with increasing nicotinamide concentration. Interestingly, the strong antioxidant melatonin did not restrain the apoptosis induced by nicotinamide in mouse myeloma cells but greatly increased the induction of nicotinamide on apoptosis. When cells were preincubated with 0.1, 1, and 10 mmol/L melatonin before nicotinamide induction, the percentage of apoptosis induced by 50 mmol/L nicotinamide markedly increased with increasing melatonin concentration. These results suggest that apoptosis induced by nicotinamide has no relationship with oxidative stress and melatonin could enhance nicotinamide-induced apoptosis in mouse myeloma cells by stimulating cell division in a certain manner. Nicotinamide may provide a new method to treat some kinds of tumors with no damage to normal tissues.
机译:通过用各种浓度的烟酰胺治疗小鼠骨髓瘤细胞(SP2 / 0)来研究烟酰胺诱导的凋亡机制。当在30,40,50和60mmol / L的浓度下用烟酰胺处理细胞处理细胞时,检测凋亡的典型标志,包括染色质缩合和DNA碎片。随着烟胺酰胺浓度的增加,凋亡率增加。有趣的是,强烈的抗氧化褪黑素没有抑制小鼠骨髓瘤细胞中烟酰胺诱导的凋亡,但大大增加了烟酰胺对凋亡的诱导。当烟酰胺诱导前用0.1,1和10mmol / L褪黑激素预孵育细胞时,随着褪黑素浓度的增加,由50mmol / L烟酰胺诱导的细胞凋亡的百分比显着增加。这些结果表明,烟酰胺诱导的细胞凋亡与氧化应激和褪黑激素的关系不能通过以某种方式刺激细胞分裂来增强小鼠骨髓瘤细胞中的烟酰胺诱导的细胞凋亡。烟酰胺可以提供一种治疗某些类型的肿瘤的新方法,对正常组织没有损伤。

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